JP6137681B2 - ニトリル化合物 - Google Patents
ニトリル化合物 Download PDFInfo
- Publication number
- JP6137681B2 JP6137681B2 JP2013145666A JP2013145666A JP6137681B2 JP 6137681 B2 JP6137681 B2 JP 6137681B2 JP 2013145666 A JP2013145666 A JP 2013145666A JP 2013145666 A JP2013145666 A JP 2013145666A JP 6137681 B2 JP6137681 B2 JP 6137681B2
- Authority
- JP
- Japan
- Prior art keywords
- fragrance
- formula
- compound represented
- composition
- nitrile compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- -1 Nitrile compounds Chemical class 0.000 title claims description 148
- 239000003205 fragrance Substances 0.000 claims description 173
- 239000000203 mixture Substances 0.000 claims description 153
- 238000000034 method Methods 0.000 claims description 53
- 238000004140 cleaning Methods 0.000 claims description 31
- 238000004519 manufacturing process Methods 0.000 claims description 27
- 239000000796 flavoring agent Substances 0.000 claims description 20
- 235000019634 flavors Nutrition 0.000 claims description 20
- 239000002304 perfume Substances 0.000 claims description 18
- 239000002537 cosmetic Substances 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 14
- 150000001299 aldehydes Chemical class 0.000 claims description 12
- 239000000835 fiber Substances 0.000 claims description 12
- 150000001298 alcohols Chemical class 0.000 claims description 8
- 230000018044 dehydration Effects 0.000 claims description 7
- 238000006297 dehydration reaction Methods 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 7
- 150000002923 oximes Chemical class 0.000 claims description 6
- 150000002170 ethers Chemical class 0.000 claims description 5
- 239000000284 extract Substances 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 150000002576 ketones Chemical class 0.000 claims description 5
- 150000002596 lactones Chemical class 0.000 claims description 5
- 239000000341 volatile oil Substances 0.000 claims description 5
- 239000002262 Schiff base Substances 0.000 claims description 4
- 150000004753 Schiff bases Chemical class 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 150000001241 acetals Chemical class 0.000 claims description 4
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 4
- 150000002825 nitriles Chemical class 0.000 claims description 4
- 150000002989 phenols Chemical class 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 229910017464 nitrogen compound Inorganic materials 0.000 claims 1
- 150000002830 nitrogen compounds Chemical class 0.000 claims 1
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 54
- 238000006243 chemical reaction Methods 0.000 description 36
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 19
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 238000002156 mixing Methods 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- 239000012043 crude product Substances 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000003513 alkali Substances 0.000 description 12
- 238000011156 evaluation Methods 0.000 description 12
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 239000003054 catalyst Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 10
- 239000010410 layer Substances 0.000 description 10
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- ACVNYUMGXUDACR-UHFFFAOYSA-N 4-(2,6,6-trimethylcyclohex-2-en-1-yl)pentanal Chemical compound O=CCCC(C)C1C(C)=CCCC1(C)C ACVNYUMGXUDACR-UHFFFAOYSA-N 0.000 description 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- 239000002585 base Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 230000002708 enhancing effect Effects 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 239000003599 detergent Substances 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- 238000004817 gas chromatography Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 6
- 235000011054 acetic acid Nutrition 0.000 description 6
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 4
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 4
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 4
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 4
- 239000012299 nitrogen atmosphere Substances 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 238000006146 oximation reaction Methods 0.000 description 4
- 238000004445 quantitative analysis Methods 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- 238000010183 spectrum analysis Methods 0.000 description 4
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 4
- NNWHUJCUHAELCL-SNAWJCMRSA-N trans-isomethyleugenol Chemical compound COC1=CC=C(\C=C\C)C=C1OC NNWHUJCUHAELCL-SNAWJCMRSA-N 0.000 description 4
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 3
- KHQDWCKZXLWDNM-KPKJPENVSA-N (e)-2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol Chemical compound CC\C(CO)=C/CC1CC=C(C)C1(C)C KHQDWCKZXLWDNM-KPKJPENVSA-N 0.000 description 3
- ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 description 3
- YPZUZOLGGMJZJO-UHFFFAOYSA-N Ambronide Chemical compound C1CC2C(C)(C)CCCC2(C)C2C1(C)OCC2 YPZUZOLGGMJZJO-UHFFFAOYSA-N 0.000 description 3
- XNBAECFIMGUCDX-UHFFFAOYSA-N CC(C#N)=CCC1=C(CCCC1(C)C)C Chemical compound CC(C#N)=CCC1=C(CCCC1(C)C)C XNBAECFIMGUCDX-UHFFFAOYSA-N 0.000 description 3
- NISORUBTNUTIGY-UHFFFAOYSA-N CC(C=NO)=CCC1=C(CCCC1(C)C)C Chemical compound CC(C=NO)=CCC1=C(CCCC1(C)C)C NISORUBTNUTIGY-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 3
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 229930002839 ionone Natural products 0.000 description 3
- 150000002499 ionone derivatives Chemical class 0.000 description 3
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 238000007086 side reaction Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 235000007586 terpenes Nutrition 0.000 description 3
- 238000005979 thermal decomposition reaction Methods 0.000 description 3
- 238000012719 thermal polymerization Methods 0.000 description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- CRDAMVZIKSXKFV-YFVJMOTDSA-N (2-trans,6-trans)-farnesol Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\CO CRDAMVZIKSXKFV-YFVJMOTDSA-N 0.000 description 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 2
- KHWTYGFHPHRQMP-UHFFFAOYSA-N (4-propan-2-ylcyclohexyl)methanol Chemical compound CC(C)C1CCC(CO)CC1 KHWTYGFHPHRQMP-UHFFFAOYSA-N 0.000 description 2
- ZCHHRLHTBGRGOT-SNAWJCMRSA-N (E)-hex-2-en-1-ol Chemical compound CCC\C=C\CO ZCHHRLHTBGRGOT-SNAWJCMRSA-N 0.000 description 2
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 2
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 2
- UFLHIIWVXFIJGU-ARJAWSKDSA-N (Z)-hex-3-en-1-ol Chemical compound CC\C=C/CCO UFLHIIWVXFIJGU-ARJAWSKDSA-N 0.000 description 2
- KGGVGTQEGGOZRN-PLNGDYQASA-N (nz)-n-butylidenehydroxylamine Chemical compound CCC\C=N/O KGGVGTQEGGOZRN-PLNGDYQASA-N 0.000 description 2
- JRJBVWJSTHECJK-LUAWRHEFSA-N (z)-3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one Chemical compound CC(=O)C(\C)=C/C1C(C)=CCCC1(C)C JRJBVWJSTHECJK-LUAWRHEFSA-N 0.000 description 2
- BVDMQAQCEBGIJR-UHFFFAOYSA-N 1-(2,2,6-trimethylcyclohexyl)hexan-3-ol Chemical compound CCCC(O)CCC1C(C)CCCC1(C)C BVDMQAQCEBGIJR-UHFFFAOYSA-N 0.000 description 2
- FVUGZKDGWGKCFE-UHFFFAOYSA-N 1-(2,3,8,8-tetramethyl-1,3,4,5,6,7-hexahydronaphthalen-2-yl)ethanone Chemical compound CC1(C)CCCC2=C1CC(C(C)=O)(C)C(C)C2 FVUGZKDGWGKCFE-UHFFFAOYSA-N 0.000 description 2
- ZHOOOLQOWQVYOE-UHFFFAOYSA-N 2-cyclohexylidene-2-phenylacetonitrile Chemical compound C=1C=CC=CC=1C(C#N)=C1CCCCC1 ZHOOOLQOWQVYOE-UHFFFAOYSA-N 0.000 description 2
- VTJWOQAFUFIQNP-UHFFFAOYSA-N 2-ethyl-4-(2,2,3-trimethylcyclopentyl)but-2-en-1-ol Chemical compound CCC(CO)=CCC1CCC(C)C1(C)C VTJWOQAFUFIQNP-UHFFFAOYSA-N 0.000 description 2
- FJCQUJKUMKZEMH-UHFFFAOYSA-N 2-methyl-4-(2,6,6-trimethylcyclohexen-1-yl)but-2-enal Chemical compound O=CC(C)=CCC1=C(C)CCCC1(C)C FJCQUJKUMKZEMH-UHFFFAOYSA-N 0.000 description 2
- MXNVWZZDDFIWHW-UHFFFAOYSA-N 2-methyl-4-(2,6,6-trimethylcyclohexen-1-yl)butanal Chemical compound O=CC(C)CCC1=C(C)CCCC1(C)C MXNVWZZDDFIWHW-UHFFFAOYSA-N 0.000 description 2
- RGHNGYANLODEHU-UHFFFAOYSA-N 2-methylbutanal;1,2,3-trimethylcyclohexene Chemical compound CCC(C)C=O.CC1CCCC(C)=C1C RGHNGYANLODEHU-UHFFFAOYSA-N 0.000 description 2
- NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 description 2
- PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 description 2
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 description 2
- CWRKZMLUDFBPAO-SREVYHEPSA-N 4-Decenal Chemical compound CCCCC\C=C/CCC=O CWRKZMLUDFBPAO-SREVYHEPSA-N 0.000 description 2
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- ZEYHEAKUIGZSGI-UHFFFAOYSA-N 4-methoxybenzoic acid Chemical compound COC1=CC=C(C(O)=O)C=C1 ZEYHEAKUIGZSGI-UHFFFAOYSA-N 0.000 description 2
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- GHBSPIPJMLAMEP-UHFFFAOYSA-N 6-pentyloxan-2-one Chemical compound CCCCCC1CCCC(=O)O1 GHBSPIPJMLAMEP-UHFFFAOYSA-N 0.000 description 2
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- 235000019568 aromas Nutrition 0.000 description 2
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- 238000009835 boiling Methods 0.000 description 2
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- 239000007795 chemical reaction product Substances 0.000 description 2
- NNWHUJCUHAELCL-UHFFFAOYSA-N cis-Methyl isoeugenol Natural products COC1=CC=C(C=CC)C=C1OC NNWHUJCUHAELCL-UHFFFAOYSA-N 0.000 description 2
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- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical group CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- ONKNPOPIGWHAQC-UHFFFAOYSA-N galaxolide Chemical compound C1OCC(C)C2=C1C=C1C(C)(C)C(C)C(C)(C)C1=C2 ONKNPOPIGWHAQC-UHFFFAOYSA-N 0.000 description 2
- IFYYFLINQYPWGJ-UHFFFAOYSA-N gamma-decalactone Chemical compound CCCCCCC1CCC(=O)O1 IFYYFLINQYPWGJ-UHFFFAOYSA-N 0.000 description 2
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Description
C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合のうちの1つは、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す。
C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合のうちの1つは、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す。
C−3’とC−2’の間の結合が、点線と共に二重結合を表し、かつ、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す(式(I−1)で表されるニトリル化合物)か、
C−2’とC−1’の間の結合が、点線と共に二重結合を表し、かつ、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す(式(I−2)で表されるニトリル化合物)か、
C−2’とC−1’の間の結合が、点線と共に二重結合を表し、かつ、C−3とC−2の間の結合が、点線と共に二重結合を表す(式(I−3)で表されるニトリル化合物)か、
または、
C−3’とC−2’の間の結合が、点線と共に二重結合を表し、かつ、C−3とC−2の間の結合が、点線と共に二重結合を表す(式(I−5)で表されるニトリル化合物)が好ましい。
本発明の式(I)で表されるニトリル化合物は、一般的な有機化学反応を用いて合成することができ、その製造方法に制限はない。本発明の式(I)で表されるニトリル化合物の製造方法としては、たとえば、式(II)で表されるオキシム化合物を脱水して式(I)で表されるニトリル化合物を得る脱水工程を有する方法が好ましい。
C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合のうちの1つは、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す。
C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合のうちの1つは、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す。
前記のように、本発明の製造方法においては、式(II)で表されるオキシム化合物を脱水して、式(I)で表されるニトリル化合物を得る工程を有する。
C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合のうちの1つは、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す。
無水酢酸法は、式(II)で表されるオキシム化合物を無水酢酸存在下、加熱により脱水して式(I)で表されるニトリル化合物を得る工程を有する。
アルカリ触媒法は、式(II)で表されるオキシム化合物をアルカリ触媒存在下、加熱により脱水して式(I)で表されるニトリル化合物を得る工程を有する。
例えば、式(III)で表されるアルデヒド化合物と、ヒドロキシルアミンとを用いてオキシム化反応を行い、式(II)で表されるオキシム化合物を得ることができる。
C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合のうちの1つは、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す。
本発明の香料組成物は、式(I)で表されるニトリル化合物を含有する。式(I)で表されるニトリル化合物の含有量は、香料組成物中、好ましくは0.01〜99質量%、より好ましくは0.1〜15質量%、更に好ましくは0.3〜3質量%である。式(I)で表されるニトリル化合物を0.01〜99質量%含むことにより、香料組成物へ香料として有用なオリス様の濃厚な甘さを持つウッディ−フローラル調の香気を付与することができる。
本発明の式(I)で表されるニトリル化合物を含有する香料組成物は、オリス様の濃厚な甘さを持つウッディ−フローラル調香気が付与され、さらに他の香料と調合することで、フローラルな甘さ強調することができる好ましい香調を有する調合香料として、各種製品の賦香成分として使用することができる。従って、本発明は、式(I)で表されるニトリル化合物を賦香成分として使用する方法、好ましくは、式(I)で表されるニトリル化合物を香料組成物、洗浄剤組成物、化粧料または繊維処理組成物の賦香成分として使用する方法である。当該化合物の使用方法としては、単独で又は他の成分と組み合わせて、石鹸、化粧品、毛髪化粧料、洗剤、柔軟剤、スプレー製品、芳香剤、香水、入浴剤等のトイレタリー製品のベースに含有させることができる。
本発明の洗浄剤組成物としては、身体用洗浄剤組成物、衣料用洗浄剤組成物、硬質表面用洗浄剤組成物が好ましく、身体用洗浄剤組成物、衣料用洗浄剤組成物がより好ましく、衣料用洗浄剤組成物が更に好ましい。
C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合のうちの1つは、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す。]
C−4とC−3間の結合は、単結合を表し、C−3とC−2の間の結合は、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す<1>に記載のニトリル化合物。
C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す<1>または<2>に記載のニトリル化合物。
C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合のうちの1つは、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す。]
C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合のうちの1つは、点線と共に二重結合を表すか、または、C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す。
〔転化率および反応収率〕
以下の製造例に示した転化率および反応収率は、内部標準法ガスクロマトグラフィー(GC)定量分析によって求めた。
<ガスクロマトグラフィーの装置及び分析条件>
GC装置:HEWLWTT PACKARD社製、型式:HP6850
カラム:J&W社製、DB−1(内径0.25mm、長さ30m、膜厚0.25μm)
キャリアガス:He、1.5mL/min
注入条件:280℃、スプリット比1/100
検出条件:FID方式、280℃
カラム温度条件:100℃→6℃/分昇温→300℃10分間保持
内部標準化合物:n−ドデカン
以下の製造例で得られた各化合物は、フーリエ変換赤外分光光度計(堀場製作所社製、型式:FT−710)、およびガスクロマトグラフ質量(GC−MS)分析計(島津製作所社製、型式:GC−2010)のスペクトル分析により同定した。測定条件等は各測定結果に記載した。
調香・香料評価業務の経験が5年以上10年未満の熟練者2名、および25年以上の熟練者3名により、におい紙法により香調と強度を判定した。におい紙(幅6mm長さ150mmの香料試験紙)の先端約5mmを、試料に浸漬し、評価した。
この蒸留留分のGC−MS分析によって、2−メチル−4−(2,6,6−トリメチル−2(1)−シクロヘキセン−1−イル)ブタナールオキシムが、4種のジアステレオマーの混合物であることを確認した。
(1)MS(EI法);m/z:223(M+),206,190,177,162,149,134,121,107,95,81,55,41。
(2)FT−IR(neat);cm-1:3226(br),2960,2913,2868,2364,2330,1657,1454,1377,939。
(3)香気:(主香気)ウッディ、(副香気)カンファー、フローラル。
(4)匂い強度:3。
(1)MS(EI法);m/z:205(M+),190,177,162,149,134,121,107,95,81,67,55,41。
(2)FT−IR(neat);cm-1:2954,2868,2362,2339,2239,1664,1454,1383,818。
(1)MS(EI法);m/z:221(M+),204,188,173,161,146,123,98,81,67,55,41。
(2)FT−IR(neat);cm-1:3290(br),2925,2866,2364,1633,1468,1360,947。
(1)MS(EI法);m/z:203(M+),188,173,160,146,123,108,93,81,67,53,41。
(2)FT−IR(neat);cm-1:2927,2866,2364,2215,1768,1629,1468,1362,1201,935。
実施例1で得られたニトリル化合物をジプロピレングリコールに90質量%の濃度で溶解し、香料組成物を調製した後、前記香気評価方法により、香気評価を行った。実施例1で得られたニトリル化合物の代わりに、実施例2で得られたニトリル化合物、セトナール(ジボダン社製)または、ボロナール(シムライズ社製)を用いて、それぞれの組成物を得た。得られたそれぞれの組成物について、香気評価を行った。得られた結果を表1に示す。
実施例1で得られた2−メチル−4−(2,6,6−トリメチル−2(1)−シクロヘキセン−1−イル)ブタンニトリル、及び実施例2で得られた2−メチル−4−(2,6,6−トリメチルシクロヘキセン−1−イル)−2−ブテンニトリルを用いて、表2に記載の配合組成になるように、香料を調合し、香料組成物を得た。
フロローサは、ジボダン社商品名、4−メチル−2−(2−メチルプロピル)テトラヒドロ−2H−4−ピラノール、
ヘリオトロピンは、高砂香料工業社商品名、3,4−メチレンジオキシベンズアルデヒド、
MDJは、花王株式会社商品名、ジヒドロジャスモン酸メチル、メチル (2−ペンチル−3−オソシクロペンチル)アセテートである。
実施例4の香料組成物は、比較例3の香料組成物に比べ、フローラル香気とバイオレット調の甘さが強まった。
実施例2で得られた2−メチル−4−(2,6,6−トリメチルシクロヘキセン−1−イル)−2−ブテンニトリルを用いて、表3に記載の配合組成になるように、香料を調合し、香料組成物を得た。
バクダノールは、IFF社商品名、2−エチル−4−(2,2,3−トリメチルシクロペン−1−イル)−2−ブテン−1−オール、
フロローサは、ジボダン社商品名、4−メチル−2−(2−メチルプロピル)テトラヒドロ−2H−4−ピラノール、
ヘリオトロピンは、高砂香料工業社商品名、3,4−メチレンジオキシベンズアルデヒド、
イソ・イースーパーは、IFF社商品名、1−(1,2,3,4,5,6,7,8−オクタヒドロ−2,3,8,8−テトラメチル−2−ナフタレニル)−エタン−1−オン、
MDJは、花王株式会社商品名、ジヒドロジャスモン酸メチル、メチル (2−ペンチル−3−オソシクロペンチル)アセテートである。
Claims (10)
- 式(I)中、C−3’とC−2’、およびC−2’とC−1’の間の結合のうち1つは、点線と共に二重結合を表し、
C−4とC−3、およびC−3とC−2の間の結合の両方が、単結合を表す請求項1に記載のニトリル化合物。 - 請求項1または2に記載のニトリル化合物を含有する香料組成物。
- 請求項1または2に記載のニトリル化合物以外の香料を更に含有する請求項3に記載の香料組成物。
- 前記ニトリル化合物以外の香料が、炭化水素類、アルコール類、フェノール類、アルデヒド類、ケトン類、アセタール類、エーテル類、エステル類、カーボネート類、ラクトン類、オキシム類、ニトリル類、シッフ塩基類、含窒素化合物、含硫黄化合物、天然精油および天然抽出物のうち1種以上を含有する、請求項4に記載の香料組成物。
- 請求項3〜5のいずれかに記載の香料組成物を含有する洗浄剤組成物。
- 請求項3〜5のいずれかに記載の香料組成物を含有する化粧料。
- 請求項3〜5のいずれかに記載の香料組成物を含有する繊維処理組成物。
- 請求項1または2に記載のニトリル化合物を賦香成分として使用する方法。
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